Analysis of epsilon germline transcripts and IL-4 mRNA expression in the adenoids suggests local IgE switching

被引:12
作者
Åström, K
Magnusson, CGM
Papatziamos, G
Hemlin, C
Scheynius, A
van der Ploeg, I [1 ]
Åström, K
机构
[1] St Eriks Hosp, Karolinska Inst, Dept Clin Sci, SE-11282 Stockholm, Sweden
[2] Karolinska Inst, Dept Med, Unit Clin Allergy Res, Stockholm, Sweden
[3] Karolinska Hosp, S-10401 Stockholm, Sweden
[4] Karolinska Inst, Dept Clin Neurosci, Unit Otorhinolaryngol, Stockholm, Sweden
[5] Karolinska Inst, Dept Med, Unit Clin Immunol & Allergy, Stockholm, Sweden
关键词
adenoids; atopy; cytokine; epsilon germline transcripts; IgE; otitis media;
D O I
10.1034/j.1398-9995.2000.00703.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 [免疫学];
摘要
Background: We have previously observed more frequent occurrence of IgE(+) and Fc epsilon RI+ cells in adenoids of atopic than nonatopic children. To investigate the hypothesis that the adenoids are involved in IgE production, we analyzed the levels of epsilon germline (epsilon GL), IL-4, and IFN-gamma transcripts in the adenoids in relation to atopy and presence of ear disease. Methods: Adenoidectomy was performed on 19 atopic and 18 nonatopic children (median age 5 years, range 2-12 years) suffering from otitis media with effusion (OME) (n = 16) or obstructive adenoids hyperplasia (AH) (n = 21). The levels of epsilon GL transcripts, IL-4, and IFN-gamma mRNA were analyzed by competitive reverse transcriptase-PCR. Results: epsilon GL transcript levels in the adenoids were found to be dependent on IL-4 mRNA expression (P < 0.01) and serum IgE levels (P < 0.05) (R-2 = 0.32, n = 37). IL-4 mRNA expression was associated with epsilon GL transcript levels (r(s) = 0.32, P = 0.05, n = 37), especially among patients with AH (r(s) = 0.53, P = 0.01, n = 21). No significant differences in IL-4 and IFN-gamma mRNA levels were observed between the groups. Conclusions: This study supports an IL-4-induced class switch to IgE production in the adenoids that might be of importance for inflammatory reactions in the upper respiratory tract.
引用
收藏
页码:1049 / 1055
页数:7
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